Methyl 4-bromo-3-carbamoylbenzoate

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Reagent Code: #203979
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CAS Number 2140305-53-7

science Other reagents with same CAS 2140305-53-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 258.07 g/mol
Formula C₉H₈BrNO₃
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MDL Number MFCD30834356
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nonsteroidal anti-inflammatory drugs (NSAIDs) and other bioactive molecules. Its functional groups—ester, bromo, and carbamoyl—allow for selective modifications, enabling the construction of complex aromatic structures. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions, where the bromine atom serves as a reactive site for carbon-carbon bond formation. Also utilized in the preparation of heterocyclic compounds through cyclization strategies, supporting research in medicinal chemistry for lead optimization and drug discovery.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,990.00
inventory 250mg
10-20 days ฿8,780.00
inventory 1g
10-20 days ฿24,850.00

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Methyl 4-bromo-3-carbamoylbenzoate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nonsteroidal anti-inflammatory drugs (NSAIDs) and other bioactive molecules. Its functional groups—ester, bromo, and carbamoyl—allow for selective modifications, enabling the construction of complex aromatic structures. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions, where the bromine atom serves as a reactive site for carbon-carbon bond formation. Also utilized in the prepar

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nonsteroidal anti-inflammatory drugs (NSAIDs) and other bioactive molecules. Its functional groups—ester, bromo, and carbamoyl—allow for selective modifications, enabling the construction of complex aromatic structures. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions, where the bromine atom serves as a reactive site for carbon-carbon bond formation. Also utilized in the preparation of heterocyclic compounds through cyclization strategies, supporting research in medicinal chemistry for lead optimization and drug discovery.

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